FDA Issues Warning about 11 Cybersecurity Vulnerabilities in IPnet Software Component

By MedTech Intelligence Staff

URGENT/11 introduces risks to medical device and hospital networks, and could allow a remote attacker to take control of a medical device such as an anesthesia machine of insulin pump.

How Are Medical Device Companies Addressing
EU MDR?

By Laura Johnson, Loftware

Label and packaging artwork processes play an important role in meeting compliance for EU MDR.

Wearables Web Seminar Focuses on Market Trends, Innovative Components and Integrating Data

By MedTech Intelligence Staff

Next week's complimentary event will give attendees insights on the market landscape and potential areas of opportunity.

Sepsis:
We Need Technologies that More Effectively Treat Patients

By Kumar Sharma, M.D.
UT Health San Antonio

Each year, more than 250,000 Americans die from the common and deadly condition.

Featured Quote

Artificial intelligence (AI) and machine learning (ML) technologies have the potential to dramatically improve patient care. Technologies that use software as a medical device (SaMD) are part of a growing industry.

— Catherine Wagner,, QAD

Combining Medical Technologies for Predictable Bone Regeneration

By Robert E. Marx, DDS,
University of Miami Miller School of Medicine

The first steps into clinically practical tissue engineering are through in-situ tissue engineering of bone.

10 Factors that Impact Injection Molding
Tooling Costs

The most expensive asset to any OEM using injection molded products is their injection molding tool, so what factors are driving the cost? This paper focuses on the ones that drive that cost up or if controlled can keep that cost down. Crescent Industries has been manufacturing injection molded tooling for over 70+ years and has a rigorous process for addressing these factors. Don’t miss out, read these factors now.

• Medical Device Audits, Certification & Verification
• Quality & Regulatory Market Access Solutions
  sponsored by UL
• Medical Device Component
  sponsored by 3M
• Medical Recall

EU MDR: REQUIREMENTS & IMPLEMENTATION

THIS EVENT WAS RECORDED JULY 17, 2019 | On Demand Webcast

This on-demand recording of the four-hour virtual event that took place July 17, 2019, conducted by leading experts on EU MDR requirements and implementation, provides concise insights into key aspects of the regulation to help companies understand and plan for the impending changes. The four hour webcast recording is $495.00

More Info

ADVANCED CAPA & ROOT CAUSE ANALYSIS

THIS EVENT WAS RECORDED MARCH 26-27, 2019

CAPA is the most critical and challenging quality system requirement in terms of complex thinking and organizational processes. How do you verify effectiveness? How can you apply project management to CAPA? What are the right data and tools for identifying trends? How do you deal with significant but infrequent problems? Should you set deadlines for closing CAPAs, and what about CAPAs that never close? What are best practices for documenting and communicating CAPA results? Not a CAPA 101 course, this workshop recording brings together leading industry CAPA process owners to discuss approaches to the most difficult problems in CAPA and root cause analysis.

More Info